Interesting facts
Interesting Facts about 4-Nitrobenzaldehyde
4-Nitrobenzaldehyde is a fascinating compound that plays a significant role in organic chemistry, particularly in the synthesis of various derivatives and products. Here are some engaging facts about this compound:
- Structural Significance: The compound features a benzene ring with a nitro group and an aldehyde functional group. This unique structure allows it to participate in a variety of chemical reactions.
- Reactivity: As an aldehyde, 4-nitrobenzaldehyde is known for its electrophilic properties, making it a prime candidate for nucleophilic addition reactions. It can react with various nucleophiles, leading to the formation of diverse functionalized compounds.
- Applications: This compound is utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its derivatives can even serve as important intermediates in organic synthesis, highlighting its versatility in chemical postulations.
- Aromatic Chemistry: The presence of the nitro group often induces *ortho* and *para* director effects in electrophilic aromatic substitution reactions. This property is essential when designing synthetic pathways for complex organic molecules.
As a testament to its importance, researchers often explore the myriad ways 4-nitrobenzaldehyde can be integrated into larger molecular constructs, driving innovation in both academia and industry. The compound is a striking example of how a simple structure can lead to complex and meaningful applications in modern chemistry.
Synonyms
4-nitrobenzaldehyde
555-16-8
p-Nitrobenzaldehyde
Benzaldehyde, 4-nitro-
p-Formylnitrobenzene
Benzaldehyde, p-nitro-
4-Nitro-benzaldehyde
4-FORMYLNITROBENZENE
para-nitrobenzaldehyde
MFCD00007346
CCRIS 1675
NSC 6103
EINECS 209-084-5
p-nitro benzaldehyde
NX859P8MB0
DTXSID5022061
CHEBI:66926
AI3-52475
NSC-6103
UNII-NX859P8MB0
NITROBENZALDEHYDE, 4-
CCRIS-1675
DTXCID402061
4-NITROBENZENECARBOXALDEHYDE
4-nitro benzaldehyde
4-Nitrobenzaldehyde; Chloramphenicol Impurity B
pNitrobenzaldehyde
pFormylnitrobenzene
4-nitrobenzaldhyde
paranitrobenzaldehyde
XXH
p-nitro-benzaldehyde
Benzaldehyde, pnitro
4-nitrobenz aldehyde
p-nitrobenzenealdehyde
Benzaldehyde, 4nitro
para-nitro benzaldehyde
(4 nitrophenyl)methanone
4NBZ
WLN: WNR DVH
4-Nitrobenzaldehyde,(S)
4-Nitrobenzaldehyde, 98%
SCHEMBL1157
CHEMBL164236
NSC6103
BCP27111
STR00898
Tox21_202930
BBL011957
STK199266
4-Nitrobenzaldehyde, p.a., 98.0%
AKOS000118887
CS-W007577
FN38101
HY-W007577
NCGC00260476-01
AC-27489
BP-11799
CAS-555-16-8
SY001417
DB-024132
N0559
NS00022368
BENZALDEHYDE,4-NITRO MFC7 H5 N1 O3
EN300-18420
BENZALDEHYDE,4-NITRO MFC7 H5 N1 O3
D70831
4-Nitrobenzaldehyde, purum, >=97.0% (HPLC)
AB-131/40217801
4-Nitrobenzaldehyde, Vetec(TM) reagent grade, 98%
Q2816679
Z57772464
F2190-0630
4-Nitrobenzaldehyde, for spectrophotometric det. of amino sugars, >=99.0%
209-084-5
Solubility of 4-nitrobenzaldehyde
4-nitrobenzaldehyde (C7H5NO3) exhibits interesting solubility characteristics that can influence its applications in various chemical processes. When considering the solubility of this compound, it is important to note the following:
As stated in solubility principles, “like dissolves like.” The presence of the nitro group contributes to the overall polarity but not enough to enhance water solubility significantly. Therefore, while it's not particularly soluble in water, its solubility in various organic solvents enables its use in different chemical syntheses and applications.
Understanding these solubility properties is crucial for effective handling and experimentation with 4-nitrobenzaldehyde in various chemical reactions.